Journal: iScience
Article Title: KNSTRN knockdown impairs autophagy flux to inhibit bladder cancer progression
doi: 10.1016/j.isci.2026.114734
Figure Lengend Snippet: KNSTRN knockdown suppresses autophagic flux in BLCA cells (A and B) T24 and 5637 cells were first transfected with mCherry-GFP-LC3 for 24 h and subsequently transfected with either si-NC or si-KNSTRN for an additional 48 h. The number of LC3 puncta (yellow for autophagosomes, red for autolysosomes) was quantified. And images were captured using a fluorescence microscope. Scale bars, 20 μm. (C) Western blot was used to determine the protein expression levels of P62. β-actin served as a control. KNSTRN-silenced and control cells were treated with either DMSO or rapamycin (Rapa, T24, 20 nM; 5637, and 50 nM) for 24 h. (D) Western blot was used to determine the protein expression levels of LC3. β-actin served as a control. KNSTRN-silenced and control cells were treated with either DMSO or chloroquine (CQ, T24, 50 μM; 5637, and 100 μM) for 24 h. Significance is determined by one-way ANOVA. Data are presented as the mean ± SD ( n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ns, not significantly different.
Article Snippet: Rapamycin (Rapa) , Selleck , Cat# S1039.
Techniques: Knockdown, Transfection, Fluorescence, Microscopy, Western Blot, Expressing, Control